| Cat.No. | Name | Information |
|---|---|---|
| M9075 | Etomoxir sodium salt | Etomoxir((R)-(+)-Etomoxir) sodium salt is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig. |
| M10566 | Valepotriate | Valepotriate has anti-epileptic and anti-cancer activities, it isolated from Valeriana jatamansi Jones. |
| M53416 | HKPao | HKPao (Hunter-killer peptide ao) is a biologically active peptide. |
| M53415 | Kp7-6 | Kp7-6, a Fas mimetic peptide, is a Fas/FasL antagonist. |
| M53414 | HXR9 | HXR9 is a cell-permeable peptide and a competitive antagonist of HOX/PBX interaction. |
| M52819 | c-JUN peptide | c-JUN peptide is a cell-permeable c-JUN-JNK interaction inhibitor. |
| M49844 | 6-Formylpterin | 6-Formylpterin is an inhibitor of Xanthine Oxidase. 6-Formylpterin induces intracellular ROS generation and apoptosis in HL-60 cells. 6-Formylpterin suppresses cell proliferation in PanC-1 cells. |
| M49505 | STAT3-IN-9 | STAT3-IN-9 is a potent STAT3 inhibitor. |
| M49504 | JAK-2/3-IN-3 | JAK-2-/3-IN-3 is a potent JAK2/3 inhibitor with IC50s of 13.00 and 14.86 nM for JAK2 and JAK3, respectively. |
| M49503 | Bozepinib | Bozepinib is a PKR (RNA-dependent protein kinase) activator and potently inhibits the HER-2 signaling pathway as well as JNK and ERK kinases. |
| M49502 | C24:1-Ceramide | C24:1-Ceramide is one of the most abundant naturally occurring ceramide. |
| M49483 | B-355252 | B-355252 is a phenoxythiophene sulfonamide small molecule and a potent NGF receptor agonist that enhances NGF-induced neurite growth. It also protects ischemic neurons from neuronal loss by attenuating DNA damage, reducing ROS production and LDH levels, and preventing neuronal apoptosis. In addition, B355252 has anti-apoptotic effects in glutamate-induced excitotoxicity and in a mouse hippocampal cell line (HT22) model of Parkinson's disease (PD). |
| M44980 | Picrasidine Q | Picrasidine Q, an alkaloid component extracted from Angelica keiskei species, has the capacity of anti-cell transformation and anti-cancer. |
| M44924 | Malvidin-3-O-galactoside chloride | Malvidin-3-galactoside chloride, an anthocyanin monomer, induces hepatocellular carcinoma (HCC) cells cycle arrest and apoptosis. |
| M44795 | Biatractylolide | Biatractylolide is a compound isolated from the ethyl acetate extract of Atractylodes macrocephala. |
| M44780 | Apioline | Apiole is an anti-tumor agent that induces apoptosis and inhibits human colon cancer cells by inducing G0/G1 cell cycle arrest. |
| M44719 | 3,6-Dihydroxyflavone | 3,6-Dihydroxyflavone is an anti-cancer agent. |
| M44673 | (E)-[6]-Dehydroparadol | (E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol (HY-14616), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cells. |
| M43377 | PI3Kδ-IN-16 | PI3Kδ-IN-16 is a potent and selective inhibitor of PI3Kδ. |
| M43376 | FD2157 | FD2157 is a photosensitive PI3K inhibitor, with IC50s of 43 nM, 83 nM, 84 nM, 14 nM for PI3Kα, PI3Kβ, PI3Kγ, PI3Kδ respectively. |
| M41359 | KWCN-41 | KWCN-41 is a selective and efficient inhibitor of RIPK1 kinase with an IC50 value of 88 nM. |
| M41313 | Angophorol | Angophorol is a flavonone compound. |
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